Abstract
Two human induced pluripotent stem cell (iPSC) lines were generated from fibroblasts of two siblings with methylmalonic acidemia cblB type carrying mutations in the MMAB gene: c.287T➔C (p.Ile96Thr) and a splicing loss-of-function variant c.584G➔A affecting the last nucleotide of exon 7 in MMAB (p.Ser174Cysfs*23). Reprogramming factors OCT3/4, SOX2, KLF4 and c-MYC were delivered using a non-integrative method based on the Sendai virus. Once established, iPSCs have shown full pluripotency, differentiation capacity and genetic stability.
Copyright © 2018 The Authors. Published by Elsevier B.V. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Alkyl and Aryl Transferases / genetics
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Amino Acid Metabolism, Inborn Errors* / genetics
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Amino Acid Metabolism, Inborn Errors* / metabolism
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Amino Acid Metabolism, Inborn Errors* / pathology
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Amino Acid Substitution
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Cellular Reprogramming Techniques*
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Female
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Humans
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Induced Pluripotent Stem Cells* / metabolism
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Induced Pluripotent Stem Cells* / pathology
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Kruppel-Like Factor 4
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Male
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Mutation, Missense*
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Transcription Factors* / biosynthesis
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Transcription Factors* / genetics
Substances
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KLF4 protein, human
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Kruppel-Like Factor 4
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Transcription Factors
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Alkyl and Aryl Transferases
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MMAB protein, human
Supplementary concepts
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Methylmalonic aciduria cblB type